Biomet SpinalPak Non-invasive Spine Fusion Stimulator System

Clinically Effective:

• Highest overall success rate in lumbar fusions - 84.7% (inclusive of ALIF, PLIF, posterolateral and combo)
• 270,000 patients treated to date
• 75% of Biomet customers are repeat prescribers

Scientifically Proven:

Pre-clinical studies have shown that Capacitive Coupling causes significantly higher levels of cellular proliferation than other electrical stimulation technologies
In vitro pre-clinical studies upregulation of multiple BMPs in as little as 30 minutes of exposure with optimal upregulation at 24 hours of exposure4

Cost Efficient:

In a double-blind study, patients experienced a 20% improvement over placebo; use of the device may reduce the need for revision surgery

Patient Compliance:

Smallest and lightest bone growth stimulation device on the market, designed with active patients in mind
Compliance monitoring, educational resources and Biomet Alerts program

Indications:

The Biomet SpinalPak Non-invasive Spine Fusion Stimulator System is a noninvasive bone growth stimulator indicated as an adjunct electrical treatment to primary lumbar spinal fusion surgery for one or two levels. - P850022/S017.

Usage:

Federal Law (U.S.A.) restricts this device to sale by or on the order of a physician. Rx Only - Prescription Only - Single Patient Use Only - Do Not Reuse.